Canonical Allele Identifier: CA442639158

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187118712T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197558T>G , CM000666.2:g.186197558T>G	GRCh38
NC_000004.11:g.187118712T>G , CM000666.1:g.187118712T>G	GRCh37
NC_000004.10:g.187355706T>G	NCBI36
NG_007965.1:g.11039T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.630T>G MANE Select	ENSP00000368079.4:p.Gly210=
ENST00000378802.4:c.630T>G	ENSP00000368079.4:p.Gly210=
ENST00000507209.5:n.1471T>G
NM_207352.3:c.630T>G	NP_997235.3:p.Gly210=
XM_005262935.2:c.630T>G	XP_005262992.1:p.Gly210=
XM_006714184.2:c.234T>G	XP_006714247.1:p.Gly78=
XM_005262935.4:c.630T>G	XP_005262992.1:p.Gly210=
XM_017008037.1:c.234T>G	XP_016863526.1:p.Gly78=
NM_207352.4:c.630T>G MANE Select	NP_997235.3:p.Gly210=